Системы ультразвуковой диагностики ALOKA ARIETTA 850
Type approval of measuring instruments · reg. No. KZ.02.01.01327-2021
Instruments of this type are listed in the GSI register of Kazakhstan and can be verified in Kazakhstan. Verification interval: 1 год.
Record data
- Registration number
- KZ.02.01.01327-2021
- Name
- Системы ультразвуковой диагностики
- Type, model
- ALOKA ARIETTA 850
- Manufacturer
- «FUJIFILM Healthcare Corporation»,
- Certificate holder
- 130640001392,Товарищество с ограниченной ответственностью Оптимус медика, ПРОСПЕКТ ГАГАРИНА, 50, КВ ОФИС 50,ГАГАРИН ДАҢҒЫЛЫ, 50, КВ КЕҢСЕ 50,+7 (727) 339 99 01,
- Type approval certificate
- 1327
- Date of issue
- 02.12.2021
- Valid until
- 02.12.2026
- Verification interval
- 1 год
- Verification procedure
- СТ РК 2.379-2015 «ГСИ РК. Аппараты ультразвуковые диагностические. Методика поверки»
Record data is shown in the original language (Russian), as in the official register.
Need verification of an instrument of this type?
We will find an accredited laboratory in your region by scope of accreditation — range and accuracy class. One request instead of calling around.
Source: GSI register of Kazakhstan, techreg.gov.kz, copy of 26.09.2026. The information is for reference — always confirm against the register and the instrument documents.